ロード中...
Functional improvement of dystrophic muscle by repression of utrophin: let-7c interaction
Duchenne muscular dystrophy (DMD) is a fatal genetic disease caused by an absence of the 427kD muscle-specific dystrophin isoform. Utrophin is the autosomal homolog of dystrophin and when overexpressed, can compensate for the absence of dystrophin and rescue the dystrophic phenotype of the mdx mouse...
保存先:
| 出版年: | PLoS One |
|---|---|
| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2017
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5646768/ https://ncbi.nlm.nih.gov/pubmed/29045431 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0182676 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|